CLASS I Drug recall · Reported 23 Sep 2020 · FDA Enforcement Report
Goldenseal Root Powder Organic recalled by Maison Terre
Maison Terre is recalling Goldenseal Root Powder Organic, Maison Terre Natural Products, www.maisonterre.net, distributed nationwide in the US. The recall was initiated on 17 Aug 2020 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1584-2020
- FDA event ID
- 86268
- Recalling firm
- Maison Terre, North Little Rock, AR
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 17 Aug 2020
- FDA classified
- 13 Sep 2020
- Reported
- 23 Sep 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Cronobacter
Timeline
| 17 Aug 2020 | Recall initiated by company | |
| 13 Sep 2020 | Classified by FDA | +27 days |
| 23 Sep 2020 | Published in enforcement report | +10 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of Non-Sterile Products: FDA laboratory analysis found product to be contaminated with various microorganisms including Enterobacter cloacae, Cronobacter sakazakii, Cronobacter dublinensis, among others.
Product as listed by the FDA
Goldenseal Root Powder Organic, 1 oz. clear plastic bag, Maison Terre Natural Products, www.maisonterre.net
Where it was distributed
Nationwide.
Questions about this recall
Why was it recalled?
Microbial Contamination of Non-Sterile Products: FDA laboratory analysis found product to be contaminated with various microorganisms including Enterobacter cloacae, Cronobacter sakazakii, Cronobacter dublinensis, among others.
Which lots are affected?
All lots distributed 01/25/2015 to 08/04/2020
Where was it sold?
Nationwide.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.